Variant #0000325171 (NC_000017.10:g.7762832C>T, NM_001080424.1:c.*5993C>T (KDM6B))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.7762832C>T
DNA change (hg38) g.7859514C>T
Published as CYB5D1(NM_144607.4):c.589C>T (p.(Arg197Trp))
ISCN -
DB-ID CYB5D1_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00182 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KDM6B NM_001080424.1 ?/. - c.*5993C>T r.(=) p.(=)
LSMD1 NM_032356.3 ?/. - c.-2091G>A r.(?) p.(=)
CYB5D1 NM_144607.4 ?/. - c.589C>T r.(?) p.(Arg197Trp)
TMEM88 NM_203411.1 ?/. - c.*3800C>T r.(=) p.(=)


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